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Research historical outbreak investigations and the full recall archive, with charts, trends, and advanced filters. Looking for what's happening right now instead? See current Health Alerts.

Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

36,950
Total recall recordsAll FDA and USDA recalls in Public Health Trace
9,732
Class I recallsReasonable probability of serious health consequences
24,263
Class II recallsTemporary or medically reversible health consequences
2,873
Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls
Most common hazardLack of Assurance of Sterility 2,071 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/made-fresh-salads-inc-recalls-ready-eat-deli-style-salads-and-cream-cheese-because-possible-healthPublished September 6, 2026
Most affected stateHawaii 200 recalls mention this state

Download matching recalls as CSV

CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.

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Recalls announced by month (Year to date)

A chart of recalls grouped by month.

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Source: FDA and USDA public dataLast updated

Summary (Year to date)

  • 1,458 recalls have been announced year to date.
  • Aug 2026 was 53% lower than the previous complete period (Jul 2026: 240).
  • The highest complete period was Jun 2026 (297).
  • Sep 2026 is incomplete and not included in the figures above.
  • Complete data
  • Incomplete
Recalls by class

A bar chart of the total number of recalls in this dataset by recall class.

Recalls by class
ClassRecalls
Class II24,263
Class I9,732
Class III2,873
Not Yet Classified1
Download CSV
Recalls by class
ClassRecalls
Class II24,263
Class I9,732
Class III2,873
Not Yet Classified1

Showing 901–920 of 17,758 recalls

FDA Recall Ongoing Historical recordClass II

Ketorolac Tromethamine Injection, USP, 60 mg/2 mL (30 mg/mL), 2 mL Single-Dose Vial, For Intramuscular Use Only, Rx only, Mfd. for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Mfd. by: ASPIRO PHARMA LIMITED, Telangana - 502281, INDIA., U.S. Contact Number: 1-866-495-1995, NDC 31722-307-25 (Carton), 31722-307-02 (Vial label).

by Aspiro Pharma Limited

Reason
Presence of Particulate Matter: Particulate matter identified as glass
Published
October 29, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Medline, Alcohol Prep Pads (2-Ply Pad, 70% Isopropyl Alcohol), 100 eaches per box, 10 boxes per case (1,000 eaches per case), Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL, 60093 USA, NDC 55329-811-30.

by Medline Industries, LP

Reason
Subpotent Drug
Published
October 29, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 %, 5 mL (0.17 FL OZ) bottles, Manufactured for: SOLA PHARMACEUTICALS LLC, Baton Rouge, LA 70810, NDC 70512-0520-05

by USV Private Limited

Reason
Failed Impurities/Degradation Specifications: The result for 'Any individual unspecified impurity' exceeds the specification limit.
Published
October 29, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Cetirizine Hydrochloride Tablets USP 10 mg, 500 Tablets bottles, Manufactured by: Unique Pharmaceuticals Labs, (A Div. of J.B. Chemicals & Pharmaceuticals, Ltd.), Mumbai 400 030, India. Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ 08816, NDC 16571-402-50

by JB Chemicals and Pharmaceuticals Ltd

Reason
Tablet/Capsules Imprinted with Wrong ID
Published
October 29, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass III

Cetirizine Hydrochloride Tablets USP 10 mg, 100 Tablets bottles, Manufactured by: Unique Pharmaceuticals Labs, (A Div. of J.B. Chemicals & Pharmaceuticals, Ltd.), Mumbai 400 030, India. Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ 08816, NDC 16571-402-10.

by JB Chemicals and Pharmaceuticals Ltd

Reason
Tablet/Capsules Imprinted with Wrong ID
Published
October 29, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Gabapentin Capsules, USP, 100 mg, 10 Capsules (10 x 1 blister pack), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-6665-61 (Blister pack), NDC 55154-3363-0 (Outer Bag).

by The Harvard Drug Group LLC

Reason
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
Published
October 29, 2025
Distribution
Nationwide

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FDA Recall Ongoing Historical recordClass II

Gabapentin Capsules, USP, 100 mg, 100 Capsules (10 x 10 blister packs), Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268, USA, NDC 0904-6665-61

by The Harvard Drug Group LLC

Reason
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
Published
October 29, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

M.C.I. Foods, Inc.

Product
Egg and Cheese Breakfast Burrito; 3.75 oz; 72 count/case; U…
Reason
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
Published
October 29, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

M.C.I. Foods, Inc.

Product
Cheese and Egg with Green Salsa Breakfast Burrito; 3.75 oz;…
Reason
Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
Published
October 29, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

DEMERS FOOD GROUP LLC

Product
Scott & Jon s Shrimp Scampi with Linguine, 9.6 oz.
Reason
Contains Linguine manufactured by Nate's Fine Foods LLC recalled for Listeria monocytogenes and implicated in ongoing outbreak
Published
October 29, 2025
Distribution
Nationwide

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FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Ready Meals Smoked Mozzarella Penne Pasta Salad, UPC 291298…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled Penne pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

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FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Smoked Mozzarella Penne Salad Kit, UPC 271876 #####. Product…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled Penne pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

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FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Ready Meals Smoked Mozzarella With Hot Links Extra Large, UP…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled Penne pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

View recall →

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Grilled Chicken & Basil Pasta Extra Large UPC 213035 #####.…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

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FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Ready Meals Basil Bowtie Pasta Salad, UPC 211913 #####. Prod…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

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FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Ready Meals Spinach Bowtie Pasta Salad, UPC 211426 #####. Pr…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

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FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Ready Meals Basil Pesto Bowtie Pasta Salad, UPC 291308 #####…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

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FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Basil Pesto Bowtie Pasta Salad, UPC 216492 #####. Product wa…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

View recall →

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
Basil Pesto Bowtie Pasta Salad, UPC 294921 #####. Product wa…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

View recall →

FDA Recall United States Terminated Historical recordClass I

Albertsons Companies LLC

Product
READY MEALS Pesto Bowtie Pasta Salad, UPC 27133 #####. Prod…
Reason
Listeria monocytogenes. Albertson's store-made deli items contain a recalled bowtie pasta ingredient which was recalled due to Listeria monocytogenes.
Published
October 29, 2025
Distribution
Distributed in AK, AR, AZ, CA, CO, HI, L…

View recall →

Data last updated:

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.